1. Mavilakandy, Akash, Ahamed, Hisham. 2022. Mutation of the MYL3 gene in a patient with mid-ventricular obstructive hypertrophic cardiomyopathy. In BMJ case reports, 15, . doi:10.1136/bcr-2021-244573. https://pubmed.ncbi.nlm.nih.gov/35288424/
2. Berge, K E, Leren, T P. 2013. Genetics of hypertrophic cardiomyopathy in Norway. In Clinical genetics, 86, 355-60. doi:10.1111/cge.12286. https://pubmed.ncbi.nlm.nih.gov/24111713/
3. Gómez, Juan, Lorca, Rebeca, Reguero, Julian R, Avanzas, Pablo, Coto, Eliecer. . Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients. In Circulation. Cardiovascular genetics, 10, . doi:10.1161/CIRCGENETICS.116.001584. https://pubmed.ncbi.nlm.nih.gov/28356264/
4. Ingles, Jodie, Goldstein, Jennifer, Thaxton, Courtney, Hershberger, Ray E, Funke, Birgit. . Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes. In Circulation. Genomic and precision medicine, 12, e002460. doi:10.1161/CIRCGEN.119.002460. https://pubmed.ncbi.nlm.nih.gov/30681346/
5. Topriceanu, Constantin-Cristian, Pereira, Alexandre C, Moon, James C, Captur, Gabriella, Ho, Carolyn Y. 2023. Meta-Analysis of Penetrance and Systematic Review on Transition to Disease in Genetic Hypertrophic Cardiomyopathy. In Circulation, 149, 107-123. doi:10.1161/CIRCULATIONAHA.123.065987. https://pubmed.ncbi.nlm.nih.gov/37929589/
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